C61
Conditions
Interventions
Group 1: Study participants work with pseudonymized micro-ultrasound images. After a baseline evaluation, all participants complete a two-day structured training program. A second evaluation after the
Sponsors
Universitätsmedizin Mannheim
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Medical students, residents, and board-certified urologists with little to no prior experience in transrectal micro-ultrasound
Exclusion criteria
Exclusion criteria: Performed or interpreted more than 40 micro-ultrasound examinations of the prostate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary Endpoint: change in pooled accuracy in detecting clinically significant prostate cancer Timepoints: before and after training intervention Data collection: Online survey for each case | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in sensitivity, specificity, receiver operating characteristic (ROC) curves, predictive values, and management recommendations | — |
Countries
Germany
Contacts
Public ContactCaelán Max Haney-Aubert
Universitätsmedizin Mannheim
Outcome results
None listed